Product Recalls in Wyoming

Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,314 recalls have been distributed to Wyoming in the last 12 months.

48,219 total recalls
2,314 in last 12 months

Showing 4104141060 of 48,219 recalls

Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra Ready Pack Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur Systems VitD 100 test Recalled by Siemens Healthcare...

The Issue: Samples containing fluorescein may show interference with the ADVIA Centaur¿...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2014· Fresenius Medical Care Holdings, Inc.

Recalled Item: Naturalyte Liquid Bicarbonate Concentrate Recalled by Fresenius Medical Care...

The Issue: Naturalyte Liquid Bicarbonate maybe contaminated

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
DrugApril 9, 2014· Nature's Universe

Recalled Item: THINOGENICS Recalled by Nature's Universe Due to Undeclared Sibutramine

The Issue: Marketed Without an Approved NDA/ANDA: Product contains undeclared sibutramine.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugApril 9, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco Pharmaceutical...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugApril 9, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Children's Cetirizine Hydrochloride Chewable Tablets Recalled by Caraco...

The Issue: Failed Impurities/Degradation Specifications: out of specification results...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 9, 2014· Cochlear Americas Inc.

Recalled Item: Cochlear Baha Soft tissue gauge 6mm. Reusable instrument used to Recalled by...

The Issue: Cochlear America is recalling Cochlear Baha Soft Tissue Gauge due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to When the E-NMT-01 module...

The Issue: When the E-NMT-01 module is used in conjunction with the ElectroSensor, the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae Recalled by...

The Issue: Potential for separation of dilator tips.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2014· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences Fem-Flex II Arterial and femoral Cannulae with Duraflo...

The Issue: Potential for separation of dilator tips.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 8, 2014· Pfizer Inc.

Recalled Item: Tikosyn¿ (dofetilide) 500 mcg (0.5mg) capsules Recalled by Pfizer Inc. Due...

The Issue: Presence of Foriegn Tablets/Capsules: A single Tikosyn¿ (dofetilide) 250 mcg...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 8, 2014· Beckman Coulter, Inc.

Recalled Item: MicroScan Pos Combo Panel Type 33 (PC33): Catalog number B1017-211 Recalled...

The Issue: Siemens investigation confirmed that a portion one lot of panel Pos Combo 33...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Siemens Medical Solutions USA, Inc.

Recalled Item: e.cam -emission computed tomography system Used to detect or image Recalled...

The Issue: There is a potential for patient finger injury on the e.cam systems.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2014· Philips Medical Systems, Inc.

Recalled Item: Intended for both adult and pediatric patients for taking diagnostic...

The Issue: In special cases, during the start-up of the current model of MobileDiagnost...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 7, 2014· Teva Pharmaceuticals USA

Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2014· Teva Pharmaceuticals USA

Recalled Item: BUPRENORPHINE HYDROCHLORIDE Sublingual Tablets Recalled by Teva...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 7, 2014· Piramal Critical Care, Inc.

Recalled Item: Sevoflurane Recalled by Piramal Critical Care, Inc. Due to Failed pH...

The Issue: Failed pH Specifications: product was too acidic.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodApril 7, 2014· Natural Grocers by Vitamin Cottage

Recalled Item: Natural Grocers by Vitamin Cottage Recalled by Natural Grocers by Vitamin...

The Issue: Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado based...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 7, 2014· Abbott Laboratories, Inc

Recalled Item: Lipase Reagent Recalled by Abbott Laboratories, Inc Due to Package inserts...

The Issue: Package inserts have incorrect SmartWash parameters for Triglyceride.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing